Comparing information for consent for orthopaedic procedures given by a video, or by a doctor, to see if this improves patient understanding of a procedure.

Not Applicable

Recruiting

• Conditions: Osteoarthritis; Hallux valgus; Joint injury; Meniscal tear; Arthritis; Cartilage disorders; Bone disease; Musculoskeletal - Osteoarthritis; Musculoskeletal - Other muscular and skeletal disorders; Surgery - Other surgery

• Registration Number: ACTRN12618001319268
• Lead Sponsor: Consentic

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-08-06
• Last Update Posted: 16 November 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 152

Inclusion Criteria

Patients aged greater than 18 years of age, who are undergoing an orthopaedic procedure, and who are able to provide informed medical consent will be invited to participate in the study.

Exclusion Criteria

Patients with visual impairment, hearing impairment, or who come from a non-English speaking background without a command of English, or do not have the capacity to consent will be excluded from participation.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Knowledge recall on a knowledge assessment scored out of ten following consent. <br>The knowledge recall has been designed specifically for this study. [Measured immediately after informed consent has been undertaken. ];Patient satisfaction recorded on a likert scale.[Measured immediately after the consent has been undertaken]

Secondary Outcome Measures

Name	Time	Method
Physician satisfaction recorded on a likert scale.[Measured immediately after the consent has been undertaken];Time per consent measured using a stopwatch [Measured in minutes and seconds from the commencement of the consent, and finishing when there are no further questions from the patient]